Society for Mucopolysaccharide Diseases (the MPS Society)
Society for Mucopolysaccharide Diseases (the MPS Society)
Fundraising

Support us through fundraising

The MPS Society supports over 1200 children and adults affected by MPS and related diseases throughout the UK, their families, carers and professionals. We provide a unique needs-led advocacy service, organise and manage events to enable those affected to come together to share experiences and learn about the latest developments in clinical management and treatment, and fund and encourage research into these devastating diseases.

But to do this we really do rely on the generosity of people like you to help us continue our vital work. You can make a difference today.

Here are some ways you can support us

Giving Money
Raising Money
Seasonal Collection
Promotional Collection
Become a Childcare Volunteer
Fundraising News
Fundraising Stories
Fundraising Resources

Get in touch

You will find lots of information on our website about how you can help but if you would like to talk to someone, please give us a call on 0845 389 9901 or email us.

Request a fundraising pack by post

To request an MPS Fundraising Pack, a School Fundraising Pack or one of our Collection Boxes by post, please call 0845 389 9901 or email us.

Fundraising Standards Board

The MPS Society is a member of the Fundraising Standards Board. The Fundraising Standards Board is a self-regulatory body, members of which agree to adhere to the highest standards of good practice in their fundraising activities. View our Fundraising Promise here. If you have a complaint regarding fundraising, we have a Fundraising Complaints Procedure available upon request.